US3880783A - Transparent moulding composition of a polycarbonate and a resin - Google Patents

Transparent moulding composition of a polycarbonate and a resin Download PDF

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Publication number
US3880783A
US3880783A US421233A US42123373A US3880783A US 3880783 A US3880783 A US 3880783A US 421233 A US421233 A US 421233A US 42123373 A US42123373 A US 42123373A US 3880783 A US3880783 A US 3880783A
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Prior art keywords
hydroxyphenyl
bis
moulding compound
rubber
transparent
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US421233A
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Volker Serini
Gert Humme
Karl-Heinz Ott
Wolfgang Cohnen
Hugo Vernaleken
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Bayer AG
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Bayer AG
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L21/00—Compositions of unspecified rubbers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00—Properties
    • C08L2201/10—Transparent films; Clear coatings; Transparent materials

Definitions

  • ABSTRACT A transparent moulding composition comprising a bisphenol polycarbonate having a low refractive index due to a content of alkyl substitution and a rubber and/or a resin.
  • This invention relates to transparent moulding compounds comprising a. 10 95 by weight of a transparent aromatic polycarbonate the linear chains of which consist to at least 50 of recurrent structural units of formula(l) R R R R 6 R R R R8 in which R which may be the same or different represent hydrogen or C, alkyl and X may represent a single bond, C to C alkylene or alkylidene or if at least one of the R substituents is a C alkyl or represents C alkylene or alkylidene if R is hydrogen and b. 5 90 by weight of a rubber and/or a transparent resin which contains rubber,
  • the invention of these moulding compounds is based on the finding that the polycarbonates defined under (a) have very. low refractive indices, so that the requirement of substantially equal refractive index with product (b) is met.
  • Polycarbonates containing recurrent units of formula (1 are known in the art. They have been described in, inter alia, Polymer Reviews, Volume 9, Chemistry and Physics of Polycarbonates, by H. Schnell, lnterscience Publisher, New York, 1964 and in German Offenlegungsschriften No. 2,063,050; 2,063,052 and 2,211,957 and in German Application No. P 22 604.3. They are basically prepared from bisphenols and phosgene in known manner. In addition to bisphenols which, when used in the synthesis of polycarbonates, yield products of formula (1), other bisphenols may also be used for the purpose of the invention to yield copolycarbonates, but these should contain at least 50% of units of formula (1).
  • Mixtures of polycarbonates which contain units of formula (1) and polycarbonates which do not contain any units of formula l) are also suitable as constituent (a) of the moulding compounds provided the mixture as a whole contains at least 50 of units of formula (1).
  • Polycarbonate units of formula 1 may be based on bisphenols such, for example, as the following:
  • Bisphenols which are carrying four alkyl substituents, i.e. in each of the 0,0,0 ,0 '-positions to the phenolic hydroxy groups are preferred, especially the following: 2,4-bis-( 3 ,5-dimethyl-4-hydroxyphenyl )-2- methylbutane and 2 ,2-bis-( 3 ,5-dimethyl-4-hydroxyphenyl )-propane.
  • the polycarbonates may, of course, be branched by incorporating small quantities of polyhydroxyl compounds, e.g. 0.05 to 2.0 mols percent (based on the quantity of bisphenols).
  • Polycarbonates of this kind have been described, e.g. in German Offenlegungsschriften No. 1,570,533; 2,116,974 and 2,113,347, in British Patents No. 885,442 and 1,079,821 and in U.S. Pat. No. 3,544,5 14.
  • polyhydroxyl compounds which are suitable for this purpose: Phloroglucinol, 4,6-dimethyl-2,4,6-tri-(4- hydroxyphenyl)-heptene-(2), 4,6-dimethyl-2,4,6-tri- (4-hydroxyphenyl )-heptane, 1 ,3 ,5-tri-(4-hydroxyphenyl)-benzene, 1,1,1-tri-(4-hydroxyphenyl)-ethane, tri-(4-hydroxyphenyl)-phenyl-methane, 2,2--bis-[4,4- (4,4-dihydroxydiphenyl)-cyclohexyl]-propane, 2,4- bis-(4-hydroxyphenyl-4-isopropyl)-phenol, 2 ,6-bis-(2- hydroxy-S '-methyl-benzyl )-4-methylphenol, 2,4- dihydroxybenzoic acid, 2-(4-hydroxyphenyl)-2-(2,4- dihydroxyphen
  • polycarbonates have molecular weights M (weight average) of 10,000 to over 200,000, preferably 20,000 to 60,000.
  • the rubbers for the purpose of this invention may be, for example, polyurethane rubbers ethylene/vinyl acetate rubbers, silicone rubbers polyether rubbers, polyalkenamer rubbers, ethylene/propylene/diene rubbers and so-called diene rubbers, i. e. hompolymers of conjugated dienes which contain from 4 to 8 carbon atoms such as butadiene, isoprene, piperylene and chloroprene, copolymers of such dienes with each other and copolymers of such dienes with other compounds, e.g. with styrene, acrylic or methacrylic compounds (e.g.
  • Rubbers which have a refractive index of n 1.50 are preferred, e.g. polybutadiene and polyisoprene, copolymers of butadiene and isoprene with styrene and acrylonitrile, and transpolypentenamers.
  • Transparent resins which contain rubber within the meaning of this invention are either transparent graft polymers into which rubber may have been mixed; transparent mixtures of graft polymers, thermoplastic resins to which rubber may be added or transparent mixtures of thermoplastic resins and rubber.
  • the total rubber content of the transparent moulding compounds according to the invention is preferably 5 to 40% by weight. It is composed of rubber which has not been grafted and which has been mixed into the transparent moulding compounds and rubber which serves as graft stock for the transparent graft polymers in the mixture.
  • Transparent graft polymers for the purpose of this invention may be obtained by grafting monomers on rubber.
  • the monomers used may be styrene and its derivatives, e.g. a-methylstyrene, a-chlorostyrene, pchlorostyrene, 2,4-dichlorostyrene, p-methylstyrene, 3,4-dimethylstyrene, oand p-divinylbenzene, p-methyl-a-methylstyrene and p-chloro-amethylstyrene, and acrylic and methyacrylic compounds, e.g.
  • acrylic and methacrylic acid acrylonitrile, methacrylonitrile, methylacrylate, ethylacrylate, npropyl and isopropyl acrylate, n-butyl and isobutylacrylate, 2-ethylhexylacrylate, methylmethacrylate, ethylmethacrylate, n-propyl and isopropylmethacrylate, nbutyl and isobutyl methacrylate, cyclohexylmethacrylate and isobornyl methacrylate and to which maleic acid anhydride may also be added.
  • Maleic acid anhydride may be used in all cases as additional monomer but not on its own.
  • the preferred monomers are styrene, a-methylstyrene, acrylonitrile, methacrylonitrile, and methyl and ethyl acrylates and methacrylates. These monomers, as well as the other monomers, may be used alone or mixed with other monomers.
  • rubbers for example, may be used as graft stock for producing the transparent graft polymers.
  • Those rubbers which have been mentioned as preferred in the above list are also preferred for this purpose,
  • Thermoplastic resins is the term used here for those polymers which can be obtained by polymerisation of one or copolymerisation of several of the above mentioned monomers which can also be used for grafting.
  • those mentioned as preferred monomers are also preferred for this purpose.
  • the rubbers, thermoplastic resins and graft polymers can be prepared by known methods of radical polymerisation, e.g. by bulk polymerisation or polymerisation in solution, suspension or emulsion or by combined process such as precipitation and bulk- /suspension processes. Polymerisation processes carried out with the aid of organometallic mixed catalysts (Ziegler-Natta catalysts) are also known.
  • the polymer mixtures of this invention may be prepared by various methods.
  • the polymers used as starting materials may all be dissolved together in a solvent or solvent mixture.
  • the polymer mixture can be obtained by precipitating all the polymers together by the addition of a non-solvent or by introducing the solution of polymers dropwise into a precipitating agent or by removal of the solvent by evaporation.
  • some polymers may be misxd separately before all the components of the composition are finally mixed.
  • latices of a resinous copolymer e.g. styrene/acrylonitrile copolymer
  • a rubber e.g. butadiene/acrylonitrile copolymer
  • the polymers used as starting materials may also be mixed in the form of solvent-free melts in mixing apparatus such as extruders, internal kneaders or mixing rollers. Mixing may also be achieved by preparing some polymers which are constituents of the mixture in the presence of other polymers, and this may be carried out in such a way that the first mentioned polymers are at least partly grafted on the high molecular weight polymers in whose presence they are prepared.
  • styrene may be polymerised by radical polymerisation in the presence of polycarbonate and polybutadiene. This polymerisation may be carried out by various known methods (solution, bead, emulsion or block polymerisation).
  • the rubber component generally forms a separate phase which is distributed in the polymer matrix.
  • the rubber may be in the form of individual globlets or several globlets agglomerated together or in the form of other regular or irregular particles or conglomerates or particles or also in the form of a network in which other polymers may be embedded.
  • the particle diameter is generally 0.01 20 pm, preferably 0.06 pm.
  • the particles may be of one or of more types differing substantially from each other in shape, size and size distribution depending on the method of preparation of the polymer mixture and the choice of its components. Due to differences in the physical make up of the rubber phases, polymer mixtures which contain the same rubber component and also have otherwise the same composition may yet differ from each other intheir properties, e.g. their toughness, weld line strength and surface gloss. Thus, for example, the surface gloss of injection mouldings is better if the rubber particles are very small than if they are coarse and, conversely, both toughness and weld line strength are greater in the case of coarser rubber particles than in the
  • Particularly high weld line strength in observed with rubber particles very irregular in size and shape, as, for example, in polymer mixtures containing non-grafted rubber.
  • Very high weld line strength is also obtained if the rubber component is a graft polymer having particle sizes of 0.8 to 10 [1,, e.g. graft made by bulk/suspension polymerisation (network structure).
  • Rubber distributed in the form of agglomerates, e. g. agglomerates of very small rubber globlets is also advantageous as it provides for excellent weld line strength and high gloss, provided the agglomerate particle size does not exceed a certain limit.
  • Total rubber content is also influencing the properties of the polymer mixtures. If two mixtures contain rubber distributed in substantially the same form, toughness and weld line strength increase with increasing rubber content while the modulus of elasticity decreases.
  • the rubber component generally forms a sepa rate phase in the polymer mixtures of this invention
  • the other polymer components of the mixture may form a common phase in which the various polymers are distributed practically in molecular dispersion, or
  • a moulding compound is defined as being transparent when a layer 1 mm in thickness has a total scattered light transmission Tp (according to DIN 5036 and DIN 4646) of at least 50. Compounds of which layers 4 mm in thickness have a Tp of at least 50 are preferred. Those which have Tp values above in layers 4 mm in thickness are particularly preferred.
  • Transparent polycarbonate based moulding compounds of the described type have not been described before.
  • Known polymer mixtures of polycarbonates based on bisphenol A and ABS polymers or butadiene/styrene polymers (high impact polystyrene) are not transparent.
  • Transparent ABS and BS graft polymers are also known but their alloys with bisphenol A based polycarbonate are not transparent because the refractive indices are very different from each other.
  • One well known condition for transparency of polyphasic polymer mixtures such as those mentioned above is substantial equality of the refractive indices of the polymer constituents. It is known to the art that polycarbonates have very high refractive indices as far as transparent thermoplastic resins are concerned. Polycarbonates previously investigated were found to have refractive indices of r1 1.56 to 1.65 (see Kunststoff-Handbuch 1972, Carl hauser Verlag, Kunststoff-V Kunststoff-Handbuch 1972, Carl hauser Verlag, Kunststoff-Handbuch 1972, Carl hauser Verlag, Kunststoff-Handbuch 1972, Carl hauser Verlag, Kunststoff-Handbuch 1972, Carl hauser Verlag, Kunststoff-Handbuch 1972, Carl hauser Verlag, Kunststoff-Handbuch 1972, Carl hauser Verlag, Kunststoff-Handbuch 1972, Carl hauser Ver
  • compositions found constitute a new class of transparent synthetic resins with a unique combination of properties not found in other transparent synthetic resins such as polystyrene, polymethylmethacrylate, polyvinyl chloride, transparent ABS and transparent polyamide, polycarbonate and polysulphone.
  • e parts by weight of the sodium salt of disproportionated abietic acid and p parts by weight of potassium persulphate are introduced into a pressure resistant vessel equipped with a stirrer.
  • the air is displaced by introducing nitrogen and the internal temperature of the vessel is adjusted to approximately 60C.
  • dodecylmercaptan r parts by weight of dodecylmercaptan are added, followed by b parts by weight of butadiene and s parts by weight of styrene.
  • thermoplastic copolymers strand delivered from the extruder was cooled and granulated.
  • TMBPA- and TMBPJ-polycarbonate from Examples la and lb were mixed with various graft polymers from The aqueous solution is heated to 65C and the air is Example 3 in weight ratios of 50 50 and 60 40, re-
  • Example 9 are described in Examples 1 to 4.
  • the polycarbonate and the other polymer components were mixed in a double screw extruder at 220 to 260C.
  • the polymer and 1d were mixed with various graft polymers from Example 3 in various weight ratios, namely 70 30, 50 50 and 40 60 via their solvent-free melt.
  • TMBPA-PC 1.546 6 1.544 yes b TMBPJ-PC 1.543 15 1.543 c TMBPJ/BPA-CPC 1.556 9 1.555
  • EXAMPLE 9 Mixtures of polycarbonates graft polymers and TMBPA-PC/BPA-PC mixture from Example 10 were mixed with mixtures of graft polymers from Example 3 and thermoplastic copolymers from Example 4, via the solvent-free melts. For details see Table 9.
  • EXAMPLE 10 Some properties of transparent TMBPA- polycarbonate/graft polymer mixtures of this invention compared with those of BPA-polycarbonate/ graft polymer mixtures
  • the polymer mixtures shown in the Table were prepared from the solvent-free melts as already described thermoplastic copolymers b Table 8 Example Polycarbonate Rubber Thermoplastic Total mixture 8 Type n 0 Run n copolymer PC/rubber/thermo- Run No. No. Example 4 mi plastic copolymer Run No.
  • Example I01- and Example l0d are comparison mixtures for comparison with mixtures Example I0 and Example ltlh.
  • a transparent moulding compound which comprises a. 10 to 95 by weight of a transparent aromatic polycarbonate the linear chains of which consist to at least 50 of recurrent structural units of for- 25 mula (1) R R R 0- X -Z;-O- C (1) R R R R in which R, to R which may be the same or different, represent hydrogen or alkyl and X represents a single bond, a C to C alkylene or alkylidene groupor H l 3 c Qf if at least one of the R to R substituents is an alkyl group or represents a C to C alkylene or alkylidene group if R to R is hydrogen and b. 5 to 90 by weight of a transparent rubber and/or a transparent resin which contains rubber, the difference in refractive indices between (a) and (b) being not more than 0.010.
  • R to R represents hydrogen or a C to C alkyl group.
  • thermoplastic resin being a homopolymer or copolymer of styrene, a-methylstyrene, acrylonitrile, methacrylonitrile, methylacrylate, methylmethacrylate, ethylacrylate or ethylmethacrylate.
  • thermoplastic resin being a homopolymer or copolymer of styrene, a-methylstyrene, acrylonitrile, methacrylonitrile, methylacrylate, methylmethacrylate, ethylacrylate or ethylmethacrylate.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polyurethanes Or Polyureas (AREA)
US421233A 1973-06-09 1973-12-03 Transparent moulding composition of a polycarbonate and a resin Expired - Lifetime US3880783A (en)

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DE2329646A DE2329646A1 (de) 1973-06-09 1973-06-09 Transparente formmassen

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JP (1) JPS5654333B2 (enrdf_load_stackoverflow)
AT (1) AT335743B (enrdf_load_stackoverflow)
AU (1) AU475655B2 (enrdf_load_stackoverflow)
BE (1) BE808229A (enrdf_load_stackoverflow)
BR (1) BR7309565D0 (enrdf_load_stackoverflow)
CA (1) CA1028787A (enrdf_load_stackoverflow)
CH (1) CH590897A5 (enrdf_load_stackoverflow)
DD (1) DD112464A5 (enrdf_load_stackoverflow)
DE (1) DE2329646A1 (enrdf_load_stackoverflow)
DK (1) DK659873A (enrdf_load_stackoverflow)
ES (1) ES421178A1 (enrdf_load_stackoverflow)
FR (1) FR2234350B1 (enrdf_load_stackoverflow)
GB (1) GB1449870A (enrdf_load_stackoverflow)
IT (1) IT1000433B (enrdf_load_stackoverflow)
NL (1) NL7316735A (enrdf_load_stackoverflow)
NO (1) NO464273L (enrdf_load_stackoverflow)
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US4105711A (en) * 1974-01-17 1978-08-08 Bayer Aktiengesellschaft PVC moulding compounds with high dimensional stability to heat
US4122131A (en) * 1977-09-14 1978-10-24 General Electric Company Polyblend composition comprising aromatic polycarbonate, polyolefin, selectively hydrogenated block copolymer and olefinic copolymer
US4145373A (en) * 1976-02-09 1979-03-20 Mobay Chemical Corporation Stress crack resistant polycarbonates
US4145374A (en) * 1977-10-27 1979-03-20 Borg-Warner Corporation High clarity blends of polycarbonates with mercaptan-modified graft polymers
US4146587A (en) * 1977-03-19 1979-03-27 Bayer Aktiengesellschaft Segment polymers derived from aromatic vinyl-diene block polymer anion and aromatic polycarbonate
US4205141A (en) * 1976-11-23 1980-05-27 Bayer Aktiengesellschaft Thermoplastic moulding compositions
US4205140A (en) * 1976-11-23 1980-05-27 Bayer Aktiengesellschaft Thermoplastic moulding compositions
US4218544A (en) * 1979-05-03 1980-08-19 The Dow Chemical Company Blends of polycarbonate with rubber and monovinylidene aromatic copolymers
US4247662A (en) * 1979-06-25 1981-01-27 General Electric Company Novel halobisphenolethylene polycarbonate-vinyl aromatic resin blends
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DE3248709A1 (de) * 1982-01-29 1983-08-04 General Electric Co., Schenectady, N.Y. Thermoplastische formmasse
US4410662A (en) * 1981-03-30 1983-10-18 Mobay Chemical Corporation Polycarbonate having an improved impact performance
US4427829A (en) 1981-03-19 1984-01-24 Teijin Chemicals, Ltd. Polycarbonate resin composition
DE3326562A1 (de) * 1982-08-02 1984-02-02 Mobay Chemical Corp., 15205 Pittsburgh, Pa. Polycarbonat-gemische mit verbesserter schlagzaehigkeit
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US4624986A (en) * 1983-04-22 1986-11-25 The Dow Chemical Company Low temperature impact resistant carbonate polymer blends
US4631311A (en) * 1984-08-21 1986-12-23 Bayer Aktiengesellschaft Acrylonitrile free blends of a polycarbonate, a graft rubber and a terpolymer resin
US4749745A (en) * 1984-02-24 1988-06-07 Montedison S.P.A. Polymeric blends based on vinyl-aromatic polymers
US5087524A (en) * 1988-09-22 1992-02-11 Mobay Corporation Article molded from a polycarbonate composition having improved platability
US5274044A (en) * 1992-07-28 1993-12-28 General Electric Company Graft copolymers containing (thioaromatic) alkyl acrylate rubber substrates
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US20070155914A1 (en) * 2006-01-05 2007-07-05 General Electric Company Polycarbonate compositions and articles formed therefrom, with matte surfaces and high light transmissions
US20100016489A1 (en) * 2004-12-21 2010-01-21 Idemitsu Kosan Co., Ltd. Aromatic polycarbonate resin composition and molding thereof
US20100160559A1 (en) * 2008-12-19 2010-06-24 Cheil Industries Inc. Polylactic Acid/Polycarbonate Resin Composition and Molded Product Made Using the Same

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DE2653145A1 (de) * 1976-11-23 1978-05-24 Bayer Ag Formmassen
WO1980000154A1 (en) * 1978-06-22 1980-02-07 Gen Electric Low melt viscosity polycarbonate compositions having improved impact strength
DE2929229A1 (de) * 1979-07-19 1981-02-12 Bayer Ag Stabilisierte thermoplastische formmassen
DE3118861A1 (de) * 1981-05-13 1982-12-02 Bayer Ag, 5090 Leverkusen "thermoplastische formmassen aus aromatischem polycarbonat und pfropfpolymerisat"
IT1199981B (it) * 1982-03-24 1989-01-05 Montedison Spa Mescole a base di polimeri vinil-aromatici
EP0103231B1 (de) 1982-09-10 1988-09-28 Bayer Ag Flammwidrige Polymermischungen
AU596309B2 (en) * 1987-06-29 1990-04-26 Idemitsu Petrochemical Co., Ltd. Polycarbonate composition
DE3721766A1 (de) * 1987-07-01 1989-01-12 Bayer Ag Mischungen aus elastomer-latices und dispersionen von aromatischen polycarbonaten, polyestern oder polyestercarbonaten sowie daraus hergestellte produkte
DE3818871A1 (de) * 1988-06-03 1989-12-14 Huels Chemische Werke Ag Thermoplastische formmassen und verfahren zu ihrer herstellung
GB8829535D0 (en) * 1988-12-19 1989-02-08 Monsanto Europe Sa Resin compositions
NL1014513C2 (nl) * 2000-02-28 2001-08-29 Dsm Nv Polymeersamenstelling bevattende een semi-kristallijn of glasvormend polymeer in een stijve fase en, als slagvastheidsverbeteraar daarin, een rubberachtig polymeer in een disperse fase.
JP6466265B2 (ja) * 2015-06-16 2019-02-06 三菱エンジニアリングプラスチックス株式会社 ポリカーボネート樹脂組成物及び成形品
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US4105711A (en) * 1974-01-17 1978-08-08 Bayer Aktiengesellschaft PVC moulding compounds with high dimensional stability to heat
US3978157A (en) * 1974-02-16 1976-08-31 Bayer Aktiengesellschaft Thermoplastic compositions comprising aromatic polycarbonate urethanes
US4145373A (en) * 1976-02-09 1979-03-20 Mobay Chemical Corporation Stress crack resistant polycarbonates
US4205141A (en) * 1976-11-23 1980-05-27 Bayer Aktiengesellschaft Thermoplastic moulding compositions
US4205140A (en) * 1976-11-23 1980-05-27 Bayer Aktiengesellschaft Thermoplastic moulding compositions
US4146587A (en) * 1977-03-19 1979-03-27 Bayer Aktiengesellschaft Segment polymers derived from aromatic vinyl-diene block polymer anion and aromatic polycarbonate
US4122131A (en) * 1977-09-14 1978-10-24 General Electric Company Polyblend composition comprising aromatic polycarbonate, polyolefin, selectively hydrogenated block copolymer and olefinic copolymer
US4145374A (en) * 1977-10-27 1979-03-20 Borg-Warner Corporation High clarity blends of polycarbonates with mercaptan-modified graft polymers
US4218544A (en) * 1979-05-03 1980-08-19 The Dow Chemical Company Blends of polycarbonate with rubber and monovinylidene aromatic copolymers
US4247662A (en) * 1979-06-25 1981-01-27 General Electric Company Novel halobisphenolethylene polycarbonate-vinyl aromatic resin blends
US4305856A (en) * 1979-07-11 1981-12-15 Sumitomo Naugatuck Co., Ltd. Thermoplastic resin composition having good heat cycle property
US4384076A (en) * 1981-01-27 1983-05-17 Teijin Chemicals Ltd. Polycarbonate resin composition having improved properties
US4427829A (en) 1981-03-19 1984-01-24 Teijin Chemicals, Ltd. Polycarbonate resin composition
US4410662A (en) * 1981-03-30 1983-10-18 Mobay Chemical Corporation Polycarbonate having an improved impact performance
US4390657A (en) * 1981-10-19 1983-06-28 General Electric Company Composition of polycarbonate, an ABS resin and an acrylate-methacrylate interpolymer
US4430475A (en) 1981-12-31 1984-02-07 Mobay Chemical Corporation Alkylated aromatic polycarbonate compositions of improved impact strength
DE3248709A1 (de) * 1982-01-29 1983-08-04 General Electric Co., Schenectady, N.Y. Thermoplastische formmasse
US4503183A (en) * 1982-01-29 1985-03-05 Martin B. Barancik Polycarbonate resin molding composition
US4478981A (en) * 1982-03-22 1984-10-23 Petrarch Systems Inc. Mixtures of polyacrylate resins and siloxane carbonate copolymers
DE3326562A1 (de) * 1982-08-02 1984-02-02 Mobay Chemical Corp., 15205 Pittsburgh, Pa. Polycarbonat-gemische mit verbesserter schlagzaehigkeit
US4448930A (en) * 1982-08-02 1984-05-15 Mobay Chemical Corporation Polycarbonate blends having an improved impact strength
US4544706A (en) * 1982-12-02 1985-10-01 The Dow Chemical Company Highly impact resistant carbonate polymer blends
US4526926A (en) * 1983-04-22 1985-07-02 The Dow Chemical Company Low gloss carbonate polymer blends
US4624986A (en) * 1983-04-22 1986-11-25 The Dow Chemical Company Low temperature impact resistant carbonate polymer blends
US4487881A (en) * 1983-10-03 1984-12-11 Mobay Chemical Corporation Impact improvement of reinforced polycarbonate/ABS blends
US4530965A (en) * 1984-02-10 1985-07-23 Atlantic Richfield Company Polymeric molding composition containing styrenic copolymer, polycarbonate and MBS polymer
US4749745A (en) * 1984-02-24 1988-06-07 Montedison S.P.A. Polymeric blends based on vinyl-aromatic polymers
US4550138A (en) * 1984-04-23 1985-10-29 Uniroyal, Inc. Polycarbonate compositions with improved low temperature impact strength
US4576991A (en) * 1984-06-25 1986-03-18 General Electric Company UV-Resistant flame retardant compositions of polycarbonates and halogenated alkenyl aromatic copolymers
US4631311A (en) * 1984-08-21 1986-12-23 Bayer Aktiengesellschaft Acrylonitrile free blends of a polycarbonate, a graft rubber and a terpolymer resin
US5087524A (en) * 1988-09-22 1992-02-11 Mobay Corporation Article molded from a polycarbonate composition having improved platability
US5274044A (en) * 1992-07-28 1993-12-28 General Electric Company Graft copolymers containing (thioaromatic) alkyl acrylate rubber substrates
US5512631A (en) * 1992-07-28 1996-04-30 General Electric Company Transparent blend compositions containing graft copolymers of (thioaromatic) alkylate rubber substrates
WO2002038675A3 (en) * 2000-11-07 2002-12-27 Gen Electric Transparent polycarbonate polyester composition and process
US20100016489A1 (en) * 2004-12-21 2010-01-21 Idemitsu Kosan Co., Ltd. Aromatic polycarbonate resin composition and molding thereof
US8299150B2 (en) * 2004-12-21 2012-10-30 Idemitsu Kosan Co., Ltd. Aromatic polycarbonate resin composition and molding thereof
US20070155914A1 (en) * 2006-01-05 2007-07-05 General Electric Company Polycarbonate compositions and articles formed therefrom, with matte surfaces and high light transmissions
US7514523B2 (en) 2006-01-05 2009-04-07 Sabic Innovative Plastics Ip B.V. Polycarbonate compositions and articles formed therefrom, with matte surfaces and high light transmissions
US20100160559A1 (en) * 2008-12-19 2010-06-24 Cheil Industries Inc. Polylactic Acid/Polycarbonate Resin Composition and Molded Product Made Using the Same
US8835558B2 (en) * 2008-12-19 2014-09-16 Cheil Industries Inc. Polylactic acid/polycarbonate resin composition and molded product made using the same

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Publication number Publication date
ATA1023673A (de) 1976-07-15
AU475655B2 (en) 1976-08-26
JPS511556A (enrdf_load_stackoverflow) 1976-01-08
NO464273L (enrdf_load_stackoverflow) 1975-01-06
DD112464A5 (enrdf_load_stackoverflow) 1975-04-12
JPS5654333B2 (enrdf_load_stackoverflow) 1981-12-24
BR7309565D0 (pt) 1974-12-31
DK659873A (enrdf_load_stackoverflow) 1975-02-03
FR2234350A1 (enrdf_load_stackoverflow) 1975-01-17
ES421178A1 (es) 1976-04-01
AT335743B (de) 1977-03-25
GB1449870A (en) 1976-09-15
AU6316973A (en) 1975-06-05
DE2329646A1 (de) 1975-01-09
IT1000433B (it) 1976-03-30
CH590897A5 (enrdf_load_stackoverflow) 1977-08-31
NL7316735A (enrdf_load_stackoverflow) 1974-12-11
SE7316433L (enrdf_load_stackoverflow) 1974-12-10
CA1028787A (en) 1978-03-28
BE808229A (fr) 1974-06-05
FR2234350B1 (enrdf_load_stackoverflow) 1978-01-06

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